Syringe Pump
by Guangdong Biolight Meditech Co., Ltd 13 variants
Ref BioFusion M300 ProModel BioFusion M300, BioFusion M300 Ex, BioFusion M300 Pro, Evadrop V20
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69325623300094X 06932562301810 | Date9 Jul 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- BioFusion M300, BioFusion M300 Ex, BioFusion M300 Pro, Evadrop V20
- Primary DI / UDI-DI
- 06932562301810
- Basic UDI-DI
- 69325623300094X
- EMDN Code
- Z12030302 Syringe pumps
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000006333
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Guangdong Biolight Meditech Co., Ltd
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Incorporates Medicinal Product: No